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Prognostic significance of HLA EMR8-5 immunohistochemically analyzed expression in osteosarcoma

BACKGROUND: Defects in Human Leukocyte Antigen (HLA) class I antigen expression and/or function in tumor cells have been extensively investigated, because of their potential role in the escape of tumor cells from T cell recognition and destruction. The researchers evaluated HLA class I expression in...

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Autores principales: Nada, Ola H, Ahmed, Naglaa S, Abou Gabal, Hoda H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987053/
https://www.ncbi.nlm.nih.gov/pubmed/24667142
http://dx.doi.org/10.1186/1746-1596-9-72
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author Nada, Ola H
Ahmed, Naglaa S
Abou Gabal, Hoda H
author_facet Nada, Ola H
Ahmed, Naglaa S
Abou Gabal, Hoda H
author_sort Nada, Ola H
collection PubMed
description BACKGROUND: Defects in Human Leukocyte Antigen (HLA) class I antigen expression and/or function in tumor cells have been extensively investigated, because of their potential role in the escape of tumor cells from T cell recognition and destruction. The researchers evaluated HLA class I expression in tumor tissue as a prognostic factor in osteosarcoma patients and as a predictor of their survival. This retrospective cohort study was conducted at the pathology laboratory of Ain Shams University Hospital, and Ain Shams University Specialized Hospital during the period between January 2009 and January 2012. METHODS: The researchers investigated HLA class I expression in primary osteosarcoma by immunohistochemistry using EMR8-5 mAbs. Furthermore, researchers evaluated the correlation between HLA class I expression and the clinicopathological status and outcome in formalin fixed paraffin embedded tissues from thirty six (36) patients with osteosarcoma. RESULTS: A high expression of HLA class I was detected in 18 (50) % of tumor samples examined; while tumors with low or negative expression represented 9 (25%) cases each. Data indicate that the overall survival rate of patients with tumors highly expressing HLA class I was significantly higher than those with low or negative expression. CONCLUSION: Down-regulation of class I antigen expression is associated with features of aggressive disease and a poorer prognosis. Therefore, it is imperative to identify HLA as a prognostic factor at the time of diagnosis to detect chemotherapy-resistant tumors and to generate a modified treatment regimen. VIRTUAL SLIDES: The virtual slides for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1159334857109547.
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spelling pubmed-39870532014-04-16 Prognostic significance of HLA EMR8-5 immunohistochemically analyzed expression in osteosarcoma Nada, Ola H Ahmed, Naglaa S Abou Gabal, Hoda H Diagn Pathol Research BACKGROUND: Defects in Human Leukocyte Antigen (HLA) class I antigen expression and/or function in tumor cells have been extensively investigated, because of their potential role in the escape of tumor cells from T cell recognition and destruction. The researchers evaluated HLA class I expression in tumor tissue as a prognostic factor in osteosarcoma patients and as a predictor of their survival. This retrospective cohort study was conducted at the pathology laboratory of Ain Shams University Hospital, and Ain Shams University Specialized Hospital during the period between January 2009 and January 2012. METHODS: The researchers investigated HLA class I expression in primary osteosarcoma by immunohistochemistry using EMR8-5 mAbs. Furthermore, researchers evaluated the correlation between HLA class I expression and the clinicopathological status and outcome in formalin fixed paraffin embedded tissues from thirty six (36) patients with osteosarcoma. RESULTS: A high expression of HLA class I was detected in 18 (50) % of tumor samples examined; while tumors with low or negative expression represented 9 (25%) cases each. Data indicate that the overall survival rate of patients with tumors highly expressing HLA class I was significantly higher than those with low or negative expression. CONCLUSION: Down-regulation of class I antigen expression is associated with features of aggressive disease and a poorer prognosis. Therefore, it is imperative to identify HLA as a prognostic factor at the time of diagnosis to detect chemotherapy-resistant tumors and to generate a modified treatment regimen. VIRTUAL SLIDES: The virtual slides for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1159334857109547. BioMed Central 2014-03-25 /pmc/articles/PMC3987053/ /pubmed/24667142 http://dx.doi.org/10.1186/1746-1596-9-72 Text en Copyright © 2014 Nada et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Nada, Ola H
Ahmed, Naglaa S
Abou Gabal, Hoda H
Prognostic significance of HLA EMR8-5 immunohistochemically analyzed expression in osteosarcoma
title Prognostic significance of HLA EMR8-5 immunohistochemically analyzed expression in osteosarcoma
title_full Prognostic significance of HLA EMR8-5 immunohistochemically analyzed expression in osteosarcoma
title_fullStr Prognostic significance of HLA EMR8-5 immunohistochemically analyzed expression in osteosarcoma
title_full_unstemmed Prognostic significance of HLA EMR8-5 immunohistochemically analyzed expression in osteosarcoma
title_short Prognostic significance of HLA EMR8-5 immunohistochemically analyzed expression in osteosarcoma
title_sort prognostic significance of hla emr8-5 immunohistochemically analyzed expression in osteosarcoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987053/
https://www.ncbi.nlm.nih.gov/pubmed/24667142
http://dx.doi.org/10.1186/1746-1596-9-72
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